Studies on A Simple Route to A Bicyclic Reserpine Intermediate

L. Gottlieb; D. Kellner; H. J.E. Loewenthal

doi:10.1080/00397918908052692

Studies on A Simple Route to A Bicyclic Reserpine Intermediate

L. Gottlieb
, D. Kellner
, H. J.E. Loewenthal

Technion-Israel Institute of Technology

Research output: Contribution to journal › Article › peer-review

7 Scopus citations

Abstract

: A concise route is described to a Reserpine synthetic inter= mediate having the features of ring E and an oxygen function for constructing ring D. This involves an unusual a-diketone cleavage, the selective elaboration of the carboxylated ring in l-naphthoic acids and selective boron halide cleavage of ester and ether groups.

Original language	English
Pages (from-to)	2987-2997
Number of pages	11
Journal	Synthetic Communications
Volume	19
Issue number	17
DOIs	https://doi.org/10.1080/00397918908052692
State	Published - Nov 1989
Externally published	Yes

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10.1080/00397918908052692

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title = "Studies on A Simple Route to A Bicyclic Reserpine Intermediate",

abstract = ": A concise route is described to a Reserpine synthetic inter= mediate having the features of ring E and an oxygen function for constructing ring D. This involves an unusual a-diketone cleavage, the selective elaboration of the carboxylated ring in l-naphthoic acids and selective boron halide cleavage of ester and ether groups.",

author = "L. Gottlieb and D. Kellner and Loewenthal, \{H. J.E.\}",

year = "1989",

month = nov,

doi = "10.1080/00397918908052692",

language = "אנגלית",

volume = "19",

pages = "2987--2997",

journal = "Synthetic Communications",

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AU - Kellner, D.

AU - Loewenthal, H. J.E.

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Y1 - 1989/11

N2 - : A concise route is described to a Reserpine synthetic inter= mediate having the features of ring E and an oxygen function for constructing ring D. This involves an unusual a-diketone cleavage, the selective elaboration of the carboxylated ring in l-naphthoic acids and selective boron halide cleavage of ester and ether groups.

AB - : A concise route is described to a Reserpine synthetic inter= mediate having the features of ring E and an oxygen function for constructing ring D. This involves an unusual a-diketone cleavage, the selective elaboration of the carboxylated ring in l-naphthoic acids and selective boron halide cleavage of ester and ether groups.

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JO - Synthetic Communications

JF - Synthetic Communications

IS - 17

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Studies on A Simple Route to A Bicyclic Reserpine Intermediate

Abstract

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